Zobrazeno 1 - 10
of 49
pro vyhledávání: '"Sheipouri A"'
Autor:
Parsaei, Mohammadamin, Sheipouri, Amirmahdi, Partovifar, Paniz, Shahriarinamin, Maryam, Sani, Sheida Mobader, Taebi, Morvarid, Arvin, Alireza
Publikováno v:
In Psychiatry Research: Neuroimaging August 2024 342
Autor:
Ayer, Anita, Fazakerley, Daniel J., Suarna, Cacang, Maghzal, Ghassan J., Sheipouri, Diba, Lee, Kevin J., Bradley, Michelle C., Fernández-del-Rio, Lucía, Tumanov, Sergey, Kong, Stephanie MY., van der Veen, Jelske N., Yang, Andrian, Ho, Joshua W.K., Clarke, Steven G., James, David E., Dawes, Ian W., Vance, Dennis E., Clarke, Catherine F., Jacobs, René L., Stocker, Roland
Publikováno v:
In Redox Biology October 2021 46
Autor:
Gallagher, Casey I., Sheipouri, Diba, Shimmon, Susan, Rawling, Tristan, Vandenberg, Robert J.
Publikováno v:
In Biochemical Pharmacology October 2020 180
Autor:
Anita Ayer, Daniel J. Fazakerley, Cacang Suarna, Ghassan J. Maghzal, Diba Sheipouri, Kevin J. Lee, Michelle C. Bradley, Lucía Fernández-del-Rio, Sergey Tumanov, Stephanie MY. Kong, Jelske N. van der Veen, Andrian Yang, Joshua W.K. Ho, Steven G. Clarke, David E. James, Ian W. Dawes, Dennis E. Vance, Catherine F. Clarke, René L. Jacobs, Roland Stocker
Publikováno v:
Redox Biology, Vol 46, Iss , Pp 102127- (2021)
Mitochondrial energy production and function rely on optimal concentrations of the essential redox-active lipid, coenzyme Q (CoQ). CoQ deficiency results in mitochondrial dysfunction associated with increased mitochondrial oxidative stress and a rang
Externí odkaz:
https://doaj.org/article/e5e37048d10e4f0db080cc6d7d4696a3
Akademický článek
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Publikováno v:
Biomolecules, Vol 10, Iss 12, p 1618 (2020)
Reduced inhibitory glycinergic neurotransmission is implicated in a number of neurological conditions such as neuropathic pain, schizophrenia, epilepsy and hyperekplexia. Restoring glycinergic signalling may be an effective method of treating these p
Externí odkaz:
https://doaj.org/article/7096e41dd773417b93697db0f7e9cac1
Autor:
Kimberley M. Reid, Robert Spaull, Smrithi Salian, Katy Barwick, Esther Meyer, Juan Zhen, Hiromi Hirata, Diba Sheipouri, Hind Benkerroum, Kathleen M. Gorman, Apostolos Papandreou, Michael A. Simpson, Yoshinobu Hirano, Irene Farabella, Maya Topf, Detelina Grozeva, Keren Carss, Martin Smith, Hardev Pall, Peter Lunt, Susanna De Gressi, Erik‐Jan Kamsteeg, Tobias B. Haack, Lucinda Carr, Rita Guerreiro, Jose Bras, Eamonn R. Maher, Richard H. Scott, Robert J. Vandenberg, F. Lucy Raymond, Wui K. Chong, Sniya Sudhakar, Kshitij Mankad, Maarten E. Reith, Philippe M. Campeau, Robert J. Harvey, Manju A. Kurian
Publikováno v:
Reid, K M, Spaull, R, Salian, S, Barwick, K, Meyer, E, Zhen, J, Hirata, H, Sheipouri, D, Benkerroum, H, Gorman, K M, Papandreou, A, Simpson, M A, Hirano, Y, Farabella, I, Topf, M, Grozeva, D, Carss, K, Smith, M, Pall, H, Lunt, P, Gressi, S D, Kamsteeg, EJ, Haack, T B, Carr, L, Guerreiro, R, Bras, J, Maher, E R, Scott, R H, Vandenberg, R J, Raymond, F L, Chong, W K, Sudhakar, S, Mankad, K, Reith, M E, Campeau, P M, Harvey, R J & Kurian, M A 2022, ' MED27, SLC6A7, and MPPE1 Variants in a Complex Neurodevelopmental Disorder with Severe Dystonia ', Movement Disorders, vol. 37, no. 10, pp. 2139-2146 . https://doi.org/10.1002/mds.29147
BackgroundDespite advances in next generation sequencing technologies, the identification of variants of uncertain significance (VUS) can often hinder definitive diagnosis in patients with complex neurodevelopmental disorders.ObjectiveThe objective o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ae6a3f384902b53907c2243d415fc8f1
https://orca.cardiff.ac.uk/id/eprint/151492/1/mds.29147.pdf
https://orca.cardiff.ac.uk/id/eprint/151492/1/mds.29147.pdf
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Fahd O Ismael, Tessa J Barrett, Diba Sheipouri, Bronwyn E Brown, Michael J Davies, Clare L Hawkins
Publikováno v:
PLoS ONE, Vol 11, Iss 12, p e0168844 (2016)
Low-density lipoprotein (LDL) is the major source of lipid within atherosclerotic lesions. Myeloperoxidase (MPO) is present in lesions and forms the reactive oxidants hypochlorous acid (HOCl) and hypothiocyanous acid (HOSCN). These oxidants modify LD
Externí odkaz:
https://doaj.org/article/5154712134ee493eac4de4dae36a5460
Publikováno v:
Molecular Pharmacology. 98:719-729
Replication studies play an essential role in corroborating research findings and ensuring that subsequent experimental works are interpreted correctly. A previously published paper indicated that the neurotransmitter glutamate, along with the compou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fe3acfbca8a898f2cac99bfb1d667671
https://doi.org/10.1124/molpharm.120.000127
https://doi.org/10.1124/molpharm.120.000127